Adalimumab Dose-Escalation Therapy Is Effective in Refractory Crohn's Disease Patients with Loss of Response to Adalimumab, Especially in Cases without Previous Infliximab Treatment.

Adalimumab dose escalation Crohn's disease Loss of response

Journal

Case reports in gastroenterology
ISSN: 1662-0631
Titre abrégé: Case Rep Gastroenterol
Pays: Switzerland
ID NLM: 101474819

Informations de publication

Date de publication:
Historique:
received: 15 11 2018
accepted: 19 12 2018
entrez: 12 6 2019
pubmed: 12 6 2019
medline: 12 6 2019
Statut: epublish

Résumé

Adalimumab dose escalation is one of the most important options in refractory Crohn's disease patients with loss of response to adalimumab. The goal of this study was to evaluate the effectiveness of adalimumab dose escalation in Crohn's disease patients with loss of response to adalimumab, since there are few reports of adalimumab dose escalation, especially in East Asia. The clinical response to adalimumab dose escalation in Crohn's disease patients with loss of response to adalimumab was evaluated retrospectively, using the Crohn's disease activity index score, serum C-reactive protein levels, and endoscopic analyses. Of the 203 Crohn's disease patients treated with anti-tumor necrosis factor, 14 refractory Crohn's disease patients with loss of response to adalimumab received adalimumab dose-escalation therapy. The C-reactive protein level was significantly reduced from the start to weeks 12 and 52 of adalimumab dose escalation in the whole group, although there were no significant reductions of Crohn's disease activity index scores. Both Crohn's disease activity index scores and C-reactive protein levels were significantly reduced from the start to weeks 12 and 52 of adalimumab dose escalation in patients without previous infliximab treatment, although C-reactive protein levels were positive in all cases with previous infliximab exposure at weeks 12 and 52. Endoscopic mucosal healing was achieved with adalimumab dose escalation in 2 cases without previous infliximab treatment. Adalimumab dose-escalation therapy is effective in refractory Crohn's disease patients with loss of response to adalimumab, especially in cases without previous infliximab treatment.

Sections du résumé

BACKGROUND/AIMS OBJECTIVE
Adalimumab dose escalation is one of the most important options in refractory Crohn's disease patients with loss of response to adalimumab. The goal of this study was to evaluate the effectiveness of adalimumab dose escalation in Crohn's disease patients with loss of response to adalimumab, since there are few reports of adalimumab dose escalation, especially in East Asia.
METHODS METHODS
The clinical response to adalimumab dose escalation in Crohn's disease patients with loss of response to adalimumab was evaluated retrospectively, using the Crohn's disease activity index score, serum C-reactive protein levels, and endoscopic analyses.
RESULTS RESULTS
Of the 203 Crohn's disease patients treated with anti-tumor necrosis factor, 14 refractory Crohn's disease patients with loss of response to adalimumab received adalimumab dose-escalation therapy. The C-reactive protein level was significantly reduced from the start to weeks 12 and 52 of adalimumab dose escalation in the whole group, although there were no significant reductions of Crohn's disease activity index scores. Both Crohn's disease activity index scores and C-reactive protein levels were significantly reduced from the start to weeks 12 and 52 of adalimumab dose escalation in patients without previous infliximab treatment, although C-reactive protein levels were positive in all cases with previous infliximab exposure at weeks 12 and 52. Endoscopic mucosal healing was achieved with adalimumab dose escalation in 2 cases without previous infliximab treatment.
CONCLUSIONS CONCLUSIONS
Adalimumab dose-escalation therapy is effective in refractory Crohn's disease patients with loss of response to adalimumab, especially in cases without previous infliximab treatment.

Identifiants

pubmed: 31182942
doi: 10.1159/000496453
pii: crg-0013-0037
pmc: PMC6547276
doi:

Types de publication

Case Reports

Langues

eng

Pagination

37-49

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Auteurs

Taketo Suzuki (T)

Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

Tsutomu Mizoshita (T)

Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

Tomoya Sugiyama (T)

Department of Gastroenterology, Aichi Medical University School of Medicine, Nagakute, Japan.

Yoshikazu Hirata (Y)

Department of Gastroenterology, Kasugai Municipal Hospital, Kasugai, Japan.

Yoshihide Kimura (Y)

Department of Gastroenterology, Nagoya City West Medical Center, Nagoya, Japan.

Yuka Suzuki (Y)

Department of Gastroenterology, Japanese Red Cross Nagoya Daini Hospital, Nagoya, Japan.
Department of Gastroenterology, Nagoya Memorial Hospital, Nagoya, Japan.

Tomonori Yamada (T)

Department of Gastroenterology, Japanese Red Cross Nagoya Daini Hospital, Nagoya, Japan.

Hironobu Tsukamoto (H)

Department of Gastroenterology, Gifu Prefectural Tajimi Hospital, Tajimi, Japan.

Takashi Mizushima (T)

Department of Gastroenterology, Gifu Prefectural Tajimi Hospital, Tajimi, Japan.

Naomi Sugimura (N)

Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

Takahito Katano (T)

Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

Satoshi Tanida (S)

Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

Hiromi Kataoka (H)

Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

Makoto Sasaki (M)

Department of Gastroenterology, Aichi Medical University School of Medicine, Nagakute, Japan.

Classifications MeSH